Artery-and vein-specific proteins and uses therefor

ABSTRACT

Arterial and venous endothelial cells are molecularly distinct from the earliest stages of angiogenesis. This distinction is revealed by expression on arterial cells of a transmembrane ligand, called EphrinB2 whose receptor EphB4 is expressed on venous cells. Targeted disruption of the EphrinB2 gene prevents the remodeling of veins from a capillary plexus into properly branched structures. Moreover, it also disrupts the remodeling of arteries, suggesting that reciprocal interactions between pre-specified arterial and venous endothelial cells are necessary for angiogenesis. This distinction can be used to advantage in methods to alter angiogenesis, methods to assess the effect of drugs on artery cells and vein cells, and methods to identify and isolate artery cells and vein cells, for example.

RELATED APPLICATIONS

This application is a continuation-in-part of PCT Application NumberPCT/US99/08098 filed Apr. 13, 1999, which is a continuation-in-part ofU.S. application Ser. No. 09/085,820 filed on May 28, 1998, which is acontinuation-in-part of U.S. application Ser. No. 09/083,546 filed onMay 22, 1998 (abandoned). This application also claims the benefit ofU.S. Provisional Application No. 60/081,757 filed on Apr. 13, 1998. Theteachings of each of these applications are incorporated herein byreference in their entirety.

BACKGROUND OF THE INVENTION

The process of blood vessel formation is fundamental in both developmentand disease. The circulatory system is the first organ system to emergeduring embryogenesis, and is necessary to nourish the developing fetus.Disorders of the circulatory system, such as coronary artery disease,are a major cause of morbidity and mortality in modern society. Thus,repairing, replacing and promoting the growth of blood vessels is amajor target of clinical research and of pharmaceutical development.Conversely, the ingrowth of new capillary networks into developingtumors is essential for the progression of cancer. Thus, the developmentof drugs that inhibit this process of tumor angiogenesis is an equallyimportant therapeutic goal. Little attention has been paid to theproblem of how arteries and veins acquire their distinct identities.Indeed, many people have assumed that the anatomical and functionaldifferences between arteries and veins simply reflect physiologicalinfluences, such as blood pressure, oxygenation and shear forces.Additional knowledge of how arteries and veins acquire their respectiveidentities would be valuable in both research and clinical settings.

SUMMARY OF THE INVENTION

The present invention relates to a method of distinguishing betweenarterial cells (including arterial endothelial cells) and venous cellsbased on the expression of a protein on arterial cells (arterialendothelial cells) and not on venous cells, and to a wide variety ofprocesses, methods and compositions of matter, including those useful inresearch and clinical settings, which are based on the difference inexpression between the two cells types. As described herein, it has beenshown that there is a molecular distinction between arterial endothelialcells (arteries) and venous endothelial cells (veins) and that arterialendothelial cells and venous endothelial cells bear molecular markerswhich can be used to identify, separate, target, manipulate or otherwiseprocess each cell type specifically (separate from the other). As aresult, arteries and veins can now be distinguished from one another,and cell types that make up arteries and veins can be assessed for othergenetic molecular or functional differences and targeted, manipulated orotherwise processed individually or separately for research, diagnosticand therapeutic purposes.

The present invention relates to methods of distinguishing andseparating arterial cells from vein cells, and more specifically,distinguishing and separating arterial endothelial cells from venousendothelial cells based on their respective molecular markers; methodsof selectively targeting or delivering drugs or agents to arteries orveins; methods of altering (enhancing or inhibiting, where “inhibiting”includes partially or completely inhibiting) the function ofartery-specific or vein-specific molecular markers or interactionbetween them (and, thus, enhancing or inhibiting the effect suchfunctions or interactions have on arterial endothelial cells or venousendothelial cells); and methods of screening for drugs which actselectively on arterial cells (and more specifically, on arterialendothelial cells) or venous cells (and more specifically, on venousendothelial cells).

The invention also relates to transgenic nonhuman mammals, such astransgenic mice, in which genes encoding an arterial cell molecularmarker or a venous cell molecular marker are altered, either physicallyor functionally, and their use as “indicator mice” to specificallyvisualize either arteries or veins, to assess the function of themolecular marker which has been altered and to identify drugs whichaffect (enhance or inhibit) their function. It further relates toantibodies which bind an arterial cell-specific marker or a venouscell-specific marker; viral or other vectors targeted to arteries orveins by virtue of their containing and expressing, respectively, anarterial cell-specific marker or a venous cell-specific marker; cDNAsuseful for preparing libraries to be screened for additional artery- orvein-specific genes, and immortalized cell lines derived from isolatedarterial endothelial cells, from venous endothelial cells, or fromtransgenic animals (e.g., mice) of the present invention.

A molecular marker for an arterial cell or a venous cell is any geneproduct (protein or RNA or combination thereof) expressed by one ofthese cell types aid not by the other. Such a marker can be arterialendothelial cell-specific (artery-specific) or venous endothelialcell-specific (vein-specific) products or proteins. In specificembodiments, these can be referred to, respectively, as arterialendothelial cell-specific (artery-specific) ligands and venousendothelial cell-specific (vein-specific receptors. Such molecularmarkers can be expressed on cell types in addition to arterial or venousendothelial cells, but are not expressed on both arterial and venousendothelial cells. Molecular markers can include, for example, mRNAs,members of ligand-receptor pairs, and any other proteins such asadhesion proteins, transcription factors or antigens which are notexpressed on both cell types. In one embodiment, the molecular marker isa membrane receptor which is the receptor for a growth factor which actson arteries or veins. In another embodiment the molecular marker is amember of an endothelial cell surface ligand-receptor pair which isexpressed on arterial or venous endothelial cells, but not on both. Forexample, as described in detail herein, a member of the Ephrin family ofligands and a member of the Eph family of receptors which is itsreceptor are molecular markers for arterial endothelial cells and venousendothelial cells, respectively and are useful to distinguish the twocell types. Any Ephrin family ligand which is expressed on arterialendothelial cells, but not on venous endothelial cells and a venousendothelial cell-specific Eph family receptor which binds the arterialendothelial cell-specific ligand can be used to distinguish betweenarteries and veins.

In one embodiment, the present invention relates to the discovery thatarterial endothelial cells express an Ephrin family ligand and venousendothelial cells express an Eph family receptor which is a receptor ofthe Ephrin family ligand expressed on the arterial endothelial cells;methods of distinguishing or separating arterial cells (arteries) fromvenous cells (veins); methods of selectively targeting or deliveringdrugs or agents to arteries or veins; methods of enhancing or inhibitingangiogenesis, including angiogenesis in tumors, such as by altering(increasing, decreasing or prolonging) activity of at least one memberof an Ephrin family ligand-cognate Eph family receptor pair and drugsuseful in the methods; and methods of screening for drugs whichselectively act on arteries or veins.

It further relates to transgenic nonhuman mammals, such as transgenicmice, which have altered genes encoding an Ephrin family ligand oraltered genes encoding an Eph family receptor, such as EphrinB2 knockoutmice which contain a tau-lacZ (tlacZ) insertion that marks arteries butnot veins or EphB4 knockout mice which contain a reporter construct(e.g., lacZ or alkaline phosphatase gene) in the EphB4 locus; methods ofusing these mice as “indicator mice” to define and visualize angiogenicprocesses (e.g., tumor angiogenesis and ischemia-associated cardiacneovascularization) or to screen drugs for their angiogenic oranti-angiogenic effects on arteries or veins in vivo; and cells, such asimmortalized cells, derived from the transgenic mice. The presentinvention also relates to antibodies which bind an artery-specificEphrin family receptor (e.g., antibodies which bind EprhinB2);antibodies which bind a venous-specific Eph family receptor (e.g.,antibodies which bind EphB4); viral or other vectors which are targetedto arteries or veins for vessel-specific gene therapy by virtue of theircontaining and expressing DNA encoding, respectively, an Ephrin familyligand (e.g., EphrinB2) or an Eph family receptor (e.g., EphB4); cDNAsuseful for preparing libraries to be screened for additionalartery-specific or vein-specific genes (whose gene products, in turn,might be artery-or vein-specific drug targets) and methods of repairingor replacing damaged arteries or veins by transplantation of isolatedarterial or venous endothelial cells, immortalized cell lines derivedfrom them, or synthetic vessels configured from these cells.

As described herein and as is known to those of skill in the art, Ephrinfamily ligands are divided into two subclasses (EphrinA and EphrinB) andEph family receptors are divided into two groups (EphA and EphB). As isalso known, within each subclass or group, individual members aredesignated by an arabic number. The invention is described herein withspecific reference to EphrinB2 and EphB4, However, other Ephrin familyligand-Eph family receptor pairs which show similar artery-andvein-specific expression and their uses are also the subject of thisinvention. Similar artery- and vein-specific pairs can be identified bymethods known to those of skill in the art.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A is a diagram of the wild type locus of the EphrinB2 gene showingthe Exon-1 structure. The filled box represents 5′ untranslated region.The hatched box starts at the ATG, and includes the signal sequence.H=HindIII; X=XbaI; N=NcoI; E=EcoRI.

FIG. 1B is a diagram of the targeting vector used to disrupt theEphrinB2 gene.

FIG. 1C is a schematic representation of the mutated EphrinB2 locus.

FIG. 2 is a bar graph indicating the binding activity to GPI-ephrin-B2of EphB2Fc in the presence of hamster anti-ephrin-B2 hybridomasupernatants.

DETAILED DESCRIPTION OF THE INVENTION

As described herein, it has been shown that arteries and veins aregenetically distinct from the earliest stages of embryonic developmentand that reciprocal interactions between arteries and veins areessential for proper vessel formation. This finding not only changesdramatically our view of the basic ontogenetic anatomy of embryonicvasculature, but also provides the means to distinguish between arterialendothelial cells and venous endothelial cells, both physically andfunctionally. As a result, means of separating the two cell types fromone another; of identifying other artery- or vein-specific genes; ofassessing the selective effects of drugs or other agents on arteries orveins and, thus, identifying those which are artery- or vein-specific;and of selectively delivering or targeting substances to either celltype, are now available. In addition, the work described herein makes itpossible to modulate (enhance or inhibit) or control vasculogenesis andangiogenesis and to do so, if desired, in an artery-specific orvein-specific manner.

As described in the examples, a gene which encodes a cellmembrane-associated ligand which is present in the nervous system andthe vascular system has been shown, in adult mice, to be expressed byarterial endothelial cells, and not by venous endothelial cells.Further, the gene which encodes the receptor for the ligands has beenshown to be expressed by venous endothelial cells, but not by arterycells. Thus, for the first time, a marker found on arterial endothelialcells (an artery-specific marker) and a venous endothelial cell-(vein-specific) marker are available, making it possible to distinguishbetween arteries and veins for a variety of purposes, such as furtherstudy and understanding of the mechanisms of blood vessel formation;selective targeting of treatments or therapies to arteries or veins(targeting to arteries but not veins or vice versa) and selectivemodulation (enhancement or inhibition) of formation, growth and survivalof arteries and/or veins.

In addition, the work presented in the examples demonstrates thatreciprocal signaling between arteries and veins is crucial for vesselmorphogenesis (development/formation of arteries and veins). Asdescribed, deletion of the ligand-encoding gene in mice prevented theproper development of both arterial and venous vessels. Since the ligandis present on arteries (but not veins), the occurrence of the venousdefect is evidence that veins require a signal from arteries for vesselmorphogenesis. Conversely, since the arteries are also defective in themutant mice, the ligand must have a function in the arterial cellsthemselves, in addition to its role in signaling to the veins. In viewof the fact the ligand present on arterial endothelial cells is atransmembrane structure, it most likely functions to receive andtransduce to arterial cells a reciprocal signal from venous cells.

Specifically, a ligand which is a member of the Ephrin family of Ephfamily receptor interactive proteins (Eph family of transmembraneligands) has been shown to be expressed by arterial endothelial cells,but not by venous endothelial cells. Thus, it is now possible todistinguish between or target arteries and veins by relying on thepresence or absence of an Ephrin family ligand and its receptor, whichis a member of the Eph family of receptor protein-tyrosine kinases. Asdescribed herein, arterial endothelial cells have been shown to expressEphrinB2 and venous endothelial cells have been shown to express EphB4,which is an EphrinB2 receptor. EphrinB2 is not expressed on venousendothelial cells and EphB4 is not expressed on arterial endothelialcells, providing a means by which the two cell types can be identifiedor distinguished and, thus, a means by which arterial endothelial cellsand venous arterial cells can be, for example, separated from oneanother, targeted specifically or acted upon in a selective manner(e.g., by a drug or agent which acts upon one cell type to the exclusionof the other). For example, antibodies that bind to EphrinB2 or to itsextracellular domain can be fluorescently labeled and allowed to bind toa mixture of cells, which are then subjected to fluorescent activatedcell sorting to select cells of arteries from the mixture.

The work described herein, particularly in the examples, refers toEphrinB2 and EphB4. However, any ligand-receptor pair from theEphrin/Eph family, any other ligand-receptor pair or any gene productproduced by one cell type and not the other (e.g., an Ephrin ligand isexpressed by arterial endothelial cells but not by venous endothelialcells and an Eph receptor is expressed by venous endothelial cells butnot by arterial endothelial cells) can be used to distinguish between oridentify and, thus, selectively act upon, arterial endothelial cells andvenous arterial cells.

The ephrins (ligands) are of two structural types, which can be furthersubdivided on the basis of sequence relationships and, functionally, onthe basis of the preferential binding they exhibit for two correspondingreceptor subgroups. Structurally, there are two types of ephrins: thosewhich are membrane-anchored by a glycerophosphatidylinositol (GPI)linkage and those anchored through a transmembrane domain.Conventionally, the ligands are divided into the Ephrin-A subclass,which are GPI-linked proteins which bind preferentially to EphAreceptors, and the ephrinB subclass, which are transmembrane proteinswhich generally bind preferentially to EphB receptors.

The Eph family receptors are a family of receptor protein-tyrosinekinases which are related to Eph, a receptor named for its expression inan erythropoietin-producing human hepatocellular carcinoma cell line.They are divided into two subgroups on the basis of the relatedness oftheir extracellular domain sequences and their ability to bindpreferentially to ephrinA proteins or ephrinB proteins. Receptors whichinteract preferentially with ephrinA proteins are EphA receptors andthose which interact preferentially with ephrinB proteins are EphBreceptors.

As used herein, the terms Ephrin and Eph are used to refer,respectively, to ligands and receptors. They can be from any of avariety of animals (e.g., mammals/nonmammals,vertebrates/nonvertebrates, including humans). The nomenclature in thisarea has changed rapidly and the terminology used herein is thatproposed as a result of work by the Eph Nomenclature Committee, whichcan be accessed, along with previously-used names at web sitehttp://www.eph-nomenclature.com. For convenience, eph receptors andtheir respective ligand(s) are given in the Table. EPH RECEPTORS ANDLIGAND SPECIFICITIES Enh Receptors Ephrins EphA1 Ephrin−A1 EphA2Ephrin−A3, −A1, A5, −A4 EphA3 Ephrin−A5, −A2, A3, −A1 EphA4 Ephrin−A5,−A1, A3, −A2, −B2, −B3 EphA5 Ephrin−A5, −A1, A2, −A3, −A4 EphA6Ephrin−A2, −A1, A3, −A4, −A5 EphA7 Ephrin−A2, −A3, A1 EpbA8 Ephrin−A5,−A3, A2 EphB1 Ephrin−B2, −B1, A3 EphB2 Ephrin−B1, −B2, B3 EphB3Ephrin−B1, −B2, B3 EphB4 Ephrin−B2, −B1 EphB5 Unknown EphB6 UnknownLigand specificines are arranged in order of decreasing affinity.Adapted from Pasquale, E. B. (1997) Curr. Opin. Cell Biol. 9(5)608.The work described herein has numerous research and clinicalapplications, which are discussed below.

As used herein, a transgenic mouse is one which has, incorporated intothe genome of some or all its nucleated cells, a genetic alterationwhich has been introduced into the mouse or at least one of itsancestors, by the manipulations of man. A transgenic mouse can result,for example, from the introduction of DNA into a fertilized mouse ovumor from the introduction of DNA into embryonic stem cells.

One embodiment of the present invention is a transgenic mouse, whichbecause of its particular genotype, expresses only in cells of veins oronly in cells of arteries a gene whose RNA transcript or polypeptidegene product can be detected, for example, by in situ hybridization ofRNA, by fluorescence, by detection of enzymatic activity, or bydetection of a gene product by antibody binding and a detection systemfor the bound antibodies.

A particular embodiment of the present invention is a transgenic mouseof genotype EphrinB2^(±), wherein the “minus” allele denotes an allelein which a naturally occurring allele has been deleted, modified orreplaced with a mutant allele, including a mutant allele which can havean insertion of an indicator gene. Such a “minus” allele can encode anEphrinB2 ligand which has wild type, altered or no ligand function. Amouse of genotype EphrinB2^(+/tlacZ) has been produced as described inExample 1 and used to demonstrate that arterial endothelial cells andvenous endothelial cells differ genetically from early stages ofdevelopment and that reciprocal interactions, essential for propercapillary bed formation, occur between the two types of vessels. Atransgenic mouse of the same phenotype can be produced by other methodsknown to those of skill in the art. Such methods are illustrated belowusing the EphrinB2 gene as an example, but can also be used for anyother vein- or artery-specific gene.

For example, it is possible to produce a vector carrying an insertion, adeletion, or one or more point mutations in the EphrinB2 gene. TheEprhinB2 transgene can be introduced into the genome, via a vectorcarrying a mutagenized EphrinB2 allele, either by introducing thetransgene into a fertilized ovum, by the method of Wagner et al., U.S.Pat. No. 4,873,191 (1989), or by introducing the transgene intoembryonic stem (ES) cells (see, for example, Capeechi, M. R., Science244:1288-1292, 1989), or by other methods.

An insertion of DNA used to construct a transgenic knockout mouse canhave within it a gene whose presence can be readily tested, such as neo,which confers upon its host cells resistance to G418. It is an advantageof an EphrinB2^(±) indicator mouse (e.g., EphrinB2^(+/taulacZ) to beable to express, under the control of the EphrinB2 promoter, anindicator gene, which can be any gene not endogenously expressed bymice. A particularly advantageous indicator gene is one whichfacilitates the detection of EphrinB2 expression, presumably as it isoccurring in the wild type allele, by the production of a gene productthat is detectable, for example, by its own light absorbance properties,its ability to act upon a substrate to yield a colored product, or itsability to bind to an indicator or dye which is itself detectable.

Further, alternative methods are available to produce conditionalknockouts or tissue specific knockouts of a gene expressed specificallyin veins or in arteries (i.e., a vein-specific or artery-specific gene),for example by a site-specific recombinase such as Cre (acting at loxPsite) or FLP1 (acting at FRT site) of yeast.

The bacteriophage P1 Cre-loxP recombination system is capable ofmediating loxP site-specific recombination in both ES cells andtransgenic mice. The site-specific recombinase Cre can also be used in apredefined cell lineage or at a certain stage of development. See, forexample, Gu, H. et al., Science 265:103-106, 1994, in which a DNApolymerase β gene segment was deleted from T cells; see also Tsien, J.Z. et al., Cell 87:1317-1326, 1996, in which Cre/loxP recombination wasrestricted to cells in the mouse forebrain.) The impact of the mutationon these cells can then be analyzed.

The Cre recombinase catalyzes recombination between 34 bp loxPrecognition sequences (Sauer, B. and Henderson, N., Proc. Natl. Acad.Sci. USA 85:5166-5170, 1988). The loxP sequences can be inserted intothe genome of embryonic stem cells by homologous recombination such thatthey flank one or more exons of a gene of interest (making a “floxed”gene). It is crucial that the insertions do not interfere with normalexpression of the gene. Mice homozygous for the floxed gene aregenerated from these embryonic stem cells by conventional techniques andare crossed to a second mouse that arbors a Cre transgene under thecontrol of a tissue type- or cell type-specific transcriptionalpromoter. In progeny that are homozygous for the floxed gene and thatcarry the Cre transgene, the floxed gene will be deleted by Cre/loxPrecombination, but only in those cell types in which the Cregene-associated promoter is active.

A gene that encodes a protein which acts to have the effect of mimickingthe phenotype caused by mutations in a vein-specific or artery-specificgene can also be used to achieve the same effect as knockouts invein-specific or artery-specific genes.

A mutation in a gene which encodes a product which prevents binding ofligand to receptor or prevents the functional consequences of suchbinding and thereby duplicates the phenotype of a vein- orartery-specific gene knockout (e.g., a dominant negative mutant) can beused as an alternative to a knockout. The mutated gene can be put underthe control of a tissue-specific promoter to be expressed in vein orartery, depending on the tissue-specific gene product whose function isto be inhibited.

In addition, one or more dominant negative alleles of an artery-specificor vein-specific gene can be put under the control of an induciblepromoter so that upon induction, the effect of the inhibition of genefunction can be studied. A dominant negative mutant can be isolated orconstructed by mutagenesis and methods to make a transgenic mouse.

Testing to identify the desired mutant or wild type alleles, or for theidentification of other alleles, can be done by PCR on isolated genomicDNA, using appropriate primers, or by Southern blots using appropriatehybridization probes, by a combination of these procedures, or by othermethods.

In addition to the uses of an indicator mouse described in the Examplesherein, one use of a mouse having an indicator gene which can markartery cells is a method for testing an effect of a drug on growth ofarteries. The method can comprise administering the drug to a mouse(e.g., embryo, neonate, juvenile, adult, a wound site, tumor, ischemiclesion or arteriovenous malformation in any of the preceding) having anindicator gene inserted in a gene specifically expressed in arteries,and observing the effect of the drug on the growth of the arteries,compared to the effect in a suitable control mouse having an indicatorgene, not treated with the drug, but maintained under identicalconditions. Similar tests may be performed on an indicator mouse havingan indicator gene which marks vein cells. The effect of the drug can be,for example, to promote growth, to inhibit growth, or to promoteaberrant growth. Administration of the drug can be by any suitable routeknown to those of skill in the art.

An indicator mouse having an indicator gene inserted in a genespecifically expressed in artery cells can be crossed with a mouse ofanother strain carrying a mutation in a gene which is to be tested forits effect on the growth and development of blood vessels, to allow foreasier visualization of the effects of the mutation specifically onartery cells. In tests similar to those described above, the effect of adrug can be assessed on the mouse which results from this type of cross,to see, for example, whether the effect of the mutation can bealleviated by the drug. In like manner, an indicator mouse having anindicator gene inserted in a gene specifically expressed in vein cellscan be used in a cross with a mouse with a mutation whose effect ongrowth of veins is to be evaluated, and the resulting hybrid used instudies of the growth of veins.

As a result of the work described herein, it is possible todifferentiate between arterial endothelial cells (arteries) and venousendothelial cells (veins) by taking advantage of the presence of anartery-specific or vein-specific gene product on the surface of thecells. Arterial endothelial cells and venous endothelial cells can eachbe isolated from cells of other tissue types by, for instance, excisionof artery or vein tissue from a sample of mammalian tissue, dissociationof the cells, allowing the cells to bind, under appropriate conditions,to a substance which has some property or characteristic (e.g., amolecule which provides a label or tag, or molecule that has affinityfor both the an artery-specific cell surface protein and another type ofmolecule) that facilitates separation of cells bound to the substancefrom cells not bound to the substance. Separation of the cells can takeadvantage of the properties of the bound substance. For example, thesubstance can be an antibody (antiserum, polyclonal or monoclonal) whichhas been raised against the protein specific to arterial endothelialcells (or to a sufficiently antigenic portion of the protein) andlabeled with a fluorochrome, with biotin, or with another label.Separation of cells bound to the substance can be by fluorescenceactivated cell sorting (FACS), for a fluorescent label, by streptavidinaffinity column, for a biotin label, by other affinity-based separationmethods, or, for example, by antibody-conjugated magnetic beads or solidsupports. “Isolated” as used herein for cells indicates that the cellshave been separated from other cell types so as to be a populationenriched for a certain cell type, compared to the starting population,and is not limited to the case of a population containing 100% one celltype.

Other means of separation can exploit, for blood vessel cells bearing anindicator insertion in a gene encoding an artery- or vein-specificprotein, the properties of the indicator gene product or portion offusion protein encoded by the indicator insertion. For example, cellsproducing an artery- or vein-specific fusion protein with a greenfluorescent protein portion or a blue fluorescent protein portion can beseparated from non-fluorescent cells by a cell sorter. Cells producing afusion protein having an artery- or vein-specific protein portion and anindicator protein or portion with binding or enzymatic activity can bedetected by the ability of the fusion protein to bind to a fluorescentsubstrate, for example a substrate for β-galactosidase or β-lactamase,or to produce a fluorescent product in cells.

The isolation of arterial endothelial cells and the isolation of venousendothelial cells allows for tests of these cell types in culture toassess the effects of various drugs, growth factors, ligands, cytokines,members of the Eph and Ephrin families of receptors and ligands,molecules that bind to cell surface proteins, or other molecules whichcan have effects on the growth and development of arteries and veins.One or more of these substances can be added to the culture medium, andthe effects of these additions can be assessed (e.g., by measurements ofgrowth rate or viability, enzyme assays, assays for the presence of cellsurface components, incorporation of labeled precursors intomacromolecules such as DNA, RNA or proteins).

Isolated arterial endothelial cells or isolated venous endothelial cellscan be maintained in artificial growth medium, and an immortalized cellline can be produced from each such isolated cell type (i.e.,“transformation”) by infection with one of any number of viruses (e.g.,retroviruses, by transduction of immortalizing oncogenes such as v-mycor SV40 T antigen) known to effectively transform cells in culture. Thevirus can be chosen for its species specificity of infectivity (e.g.,murine ecotropic virus for mouse cells; amphotropic or pseudotypedviruses for human cells). As an alternative to viral transformation,cells can be maintained in culture by propagating the cells in mediumcontaining one or more growth factors.

Immortalized cell lines derived from either vein or artery cells can beused to produce cDNA libraries to facilitate study of genes activelyexpressed in each of these tissues. Further, such cell lines can be usedto isolate and identify proteins expressed in the cells, for instance,by purifying the proteins from conditioned growth medium or from thecells themselves.

As one alternative to using immortalized cell lines of arterial orvenous origin, cells or cell lines of non-arterial origin or non-venousorigin (e.g., endothelial cells from other tissues, or fibroblasts) canbe genetically altered (by the introduction of one or morenon-endogenously expressed genes) to express an artery-specific orvein-specific cell surface protein, and used in methods to detect andidentify substances that interfere with receptor-ligand interaction.

Introduction of one or more genes into a cell line can be, for instance,by transformation, such as by electroporation, by calcium phosphate,DEAE-dextran, or by liposomes, using a vector which has been constructedto have an insertion of one or more genes. See Ausubel, F. M. et al,Current Protocols in Molecular Biology, chapter 9, containingsupplements through Supplement 40, Fall, 1997, John Wiley & Sons, NewYork. The introduction of one or more genes to be expressed in a cellline can also be accomplished by viral infection, for example, by aretrovirus. Retroviral gene transfer has been used successfully tointroduce genes into whole cell populations, thereby eliminatingproblems associated with clonal variation.

The ability to differentiate and to isolate the cells of veins andarteries allows for a wide variety of applications for a wide variety ofpurposes. For example, it is now possible to assess the effects ofvarious agents, such as drugs, diagnostic reagents andenvironmental/dietary factors, on arteries and veins and to determine ifthe effects observed are common to both types of cells or specific toone cell type.

For example, it can no longer be assumed that angiogenic andanti-angiogenic factors or drugs act equivalently on arterial and venouscells. Isolation of these cell types of these tissues, which is madepossible by the present work, allows testing of these angiogenic andanti-angiogenic factors for arterial or venous specificity, which willprovide more selective clinical indications for these drugs. It willalso allow the discovery of new artery- or vein-selective drugs, such asby high-throughput screening of immortalized arterial or venousendothelial cell lines. Existing drugs can also be selectively targetedto arteries or veins by using the proteins described herein as targetingdevices (e.g., liposomes or viral vehicles having the protein or anextracellular domain portion thereof on the viral surface) to deliverdrugs (e.g., chemically coupled drugs) to one type of vessel or theother. For example, artery-specific agents can be used to promotecollateral growth of arteries to bypass coronary artery occlusions orischemic lesions.

There are numerous approaches to screening agents for their selectiveeffects (angiogenic or anti-angiogenic, affecting vasotension, orinhibiting formation of atherosclerotic plaques) on arteries and veins.For example, high-throughput screening of compounds or molecules can becarried out to identify agents or drugs which act selectively onarteries or veins or, in some cases, on both. Test agents to be assessedfor their effects on artery or vein cells can be any chemical (element,molecule, compound), made synthetically, made by recombinant techniquesor isolated from a natural source. For example, test agents can bepeptides, polypeptides, peptoids, sugars, hormones, or nucleic acidmolecules, such as antisense nucleic acid molecules. In addition, testagents can be small molecules or molecules of greater complexity made bycombinatorial chemistry, for example, and compiled into libraries. Theselibraries can comprise, for example, alcohols, alkyl halides, amines,amides, esters, aldehydes, ethers and other classes of organiccompounds. Test agents can also be natural or genetically engineeredproducts isolated from lysates or growth media of cells—bacterial,animal or plant—or can be the cell lysates or growth media themselves.Presentation of test compounds to the test system can be in either anisolated form or as mixtures of compounds, especially in initialscreening steps.

The compounds or molecules (referred to collectively as agents or drugs)which are screened can be those already known to have angiogenic,anti-angiogenic activity, anti-plaque activity or vasoactivity, or thoseof unknown effectiveness. In the case of those agents of known effect,the screening will be useful to identify those drugs which actselectively on arterial endothelial cells or on venous endothelialcells. In the case of those agents of unknown effect, screening will beuseful to newly identify drugs which have angiogenic, antiangiogenicactivity, anti-plaque activity or vasoactivity, and to establish thecell type (arterial, venous) on which they act. For example,immortalized cell lines of arterial or venous origin can be used toscreen libraries of compounds to identify drugs with artery- orvein-specific drug effects.

In one embodiment, an assay can be carried out to screen for drugs thatspecifically inhibit binding of an Ephrin ligand to its Eph receptor,such as binding of EphrinB2 to the EphB4 receptor, or vice-versa, byinhibition of binding of labeled ligand- or receptor-Fc fusion proteinsto immortalized cells. Alternatively, such libraries can be screened toidentify members which enhance binding of an Ephrin ligand to its Ephreceptor by enhancing binding of labeled ligand- or receptor-Fc fusionproteins to immortalized cells. Drugs identified through this screeningcan then be tested in animal models (e.g., models of cancer,arteriovenous malformations or coronary artery disease) to assess theiractivity in vivo.

A drug that inhibits interaction of an artery-specific cell surfacemolecule (e.g., an arterial endothelial cell-specific surface molecule)with a vein-specific cell surface molecule (e.g., a veinous endothelialcell-specific surface molecule) can be identified by a method in which,for example, the arterial endothelial cell-specific surface molecule andthe venous endothelial cell-specific surface molecule are combined witha drug to be assessed for its ability to inhibit interaction between thecell-specific molecules, under conditions appropriate for interactionbetween the cell-specific molecules. The cell-specific molecules may beused in the assay such that both are found on intact cells in suspension(e.g., isolated arterial or venous endothelial cells, immortalized cellsderived from these, or cells which have been modified to express anartery- or vein-specific cells surface molecule); one cell type is fixedto a solid support, and the other molecule specific to the other celltype is in soluble form in a suitable solution; or the molecule specificto one cell type is fixed to a solid support while the molecule specificto the other cell type is found free in a solution that allows forinteraction of the cell-specific molecules. Other variations arepossible to allow for the convenient assessment of the interactionbetween the two different cell-specific molecules.

In further steps of the assay, the extent to which the cell-specificmolecules interact is determined, in the presence of the drug, and in aseparate test (control), in the absence of the drug. The extent to whichinteraction of the cell-specific molecules occurs in the presence and inthe absence of the drug to be assessed is compared. If the extent towhich interaction of the cell-specific molecules occurs is less in thepresence of the drug than in the absence of the drug, the drug is onewhich inhibits interaction of the arterial endothelial cell-specificmolecule with the venous endothelial cell-specific molecule. If theextent to which interaction of the cell-specific molecules occurs isgreater in the presence of the drug than in the absence of the drug, thedrug is one which enhances interaction of the arterial endothelialcell-specific molecule with the venous endothelial cell-specificmolecule.

In one embodiment of an assay to identify a substance that interfereswith interaction of two cell surface molecules, one specific to arteryand the other specific to vein (e.g., binding of a ligand to a receptorthat recognizes it; interaction between adhesion proteins; interactionbetween a cell surface protein and a carbohydrate moiety on a cellsurface), samples of cells expressing one type of cell surface molecule(e.g., cells expressing an Eph receptor, such as a a vein-derived cellline or other cells genetically manipulated to express the Eph receptor)are contacted with either labeled ligand (e.g., an ephrin ligand, asoluble portion thereof, or a soluble fusion protein such as a fusion ofthe extracellular domain and the Fc domain of IgG) or labeled ligandplus a test compound or group of test compounds. The amount of labeledligand which has bound to the cells is determined. A lesser amount oflabel (where the label can be, for example, a radioactive isotope, afluorescent or colormetric label) in the sample contacted with the testcompound(s) is an indication that the test compound(s) interferes withbinding. The reciprocal assay using cells expressing a ligand (e.g., anEphrin ligand or a soluble form thereof) can be used to test for asubstance that interferes with the binding of a receptor or solubleportion thereof.

An assay to identify a substance which interferes with interactionbetween artery-specific and vein-specific cell surface protein can beperformed with the component (e.g., cells, purified protein, includingfusion proteins and portions having binding activity) which is not to bein competition with a test compound, linked to a solid support. Thesolid support can be any suitable solid phase or matrix, such as a bead,the wall of a plate or other suitable surface (e.g., a well of amicrotiter plate), column pore glass (CPG) or a pin that can besubmerged into a solution, such as in a well. Linkage of cells orpurified protein to the solid support can be either direct or throughone or more linker molecules.

Upon the isolation from a mammal of a gene expressing an artery-specificor a vein-specific protein, the gene can be incorporated into anexpression system for production of a recombinant protein or fusionprotein, followed by isolation and testing of the protein in vitro. Theisolated or purified protein can also be used in further structuralstudies that allow for the design of agents which specifically bind tothe protein and can act as agonists or antagonists of the receptor orligand activity of the protein.

In one embodiment, an isolated or purified artery-specific orvein-specific protein can be immobilized on a suitable affinity matrixby standard techniques, such as chemical cross-linking, or via anantibody raised against the isolated or purified protein, and bound to asolid support. The matrix can be packed in a column or other suitablecontainer and is contacted with one or more compounds (e.g., a mixture)to be tested under conditions suitable for binding of the compound tothe protein. For example, a solution containing compounds can be made toflow through the matrix. The matrix can be washed with a suitable washbuffer to remove unbound compounds and non-specifically bound compounds.Compounds which remain bound can be released by a suitable elutionbuffer. For example, a change in the ionic strength or pH of the elutionbuffer can lead to a release of compounds. Alternatively, the elutionbuffer can comprise a release component or components designed todisrupt binding of compounds (e.g., one or more ligands or receptors, asappropriate, or analogs thereof which can disrupt binding orcompetitively inhibit binding of test compound to the protein).

Fusion proteins comprising all of, or a portion of, an artery-specificor a vein-specific protein linked to a second moiety not occurring inthat protein as found in nature can be prepared for use in anotherembodiment of the method. Suitable fusion proteins for this purposeinclude those in which the second moiety comprises an affinity ligand(e.g., an enzyme, antigen, epitope). The fusion proteins can be producedby the insertion of a gene specifically expressed in artery or veincells or a portion thereof into a suitable expression vector, whichencodes an affinity ligand. The expression vector can be introduced intoa suitable host cell for expression. Host cells are disrupted and thecell material, containing fusion protein, can be bound to a suitableaffinity matrix by contacting the cell material with an affinity matrixunder conditions sufficient for binding of the affinity ligand portionof the fusion protein to the affinity matrix.

In one aspect of this embodiment, a fusion protein can be immobilized ona suitable affinity matrix under conditions sufficient to bind theaffinity ligand portion of the fusion protein to the matrix, and iscontacted with one or more compounds (e.g., a mixture) to be tested,under conditions suitable for binding of compounds to the receptor orligand protein portion of the bound fusion protein. Next, the affinitymatrix with bound fusion protein can be washed with a suitable washbuffer to remove unbound compounds and non-specifically bound compoundswithout significantly disrupting binding of specifically boundcompounds. Compounds which remain bound can be released by contactingthe affinity matrix having fusion protein bound thereto with a suitableelution buffer (a compound elution buffer). In this aspect, compoundelution buffer can be formulated to permit retention of the fusionprotein by the affinity matrix, but can be formulated to interfere withbinding of the compound(s) tested to the receptor or ligand proteinportion of the fusion protein. For example, a change in the ionicstrength or pH of the elution buffer can lead to release of compounds,or the elution buffer can comprise a release component or componentsdesigned to disrupt binding of compounds to the receptor or ligandprotein portion of the fusion protein (e.g., one or more ligands orreceptors or analogs thereof which can disrupt binding of compounds tothe receptor or ligand protein portion of the fusion protein).

Immobilization can be performed prior to, simultaneous with, or aftercontacting the fusion protein with compound, as appropriate. Variouspermutations of the method are possible, depending upon factors such asthe compounds tested, the affinity matrix selected, and elution bufferformulation. For example, after the wash step, fusion protein withcompound bound thereto can be eluted from the affinity matrix with asuitable elution buffer (a matrix elution buffer). Where the fusionprotein comprises a cleavable linker, such as a thrombin cleavage site,cleavage from the affinity ligand can release a portion of the fusionwith compound bound thereto. Bound compound can then be released fromthe fusion protein or its cleavage product by an appropriate method,such as extraction.

One or more compounds can be tested simultaneously according to themethod. Where a mixture of compounds is tested, the compounds selectedby the foregoing processes can be separated (as appropriate) andidentified by suitable methods (e.g., PCR, sequencing, chromatography).Large combinatorial libraries of compounds (e.g., organic compounds,peptides, nucleic acids) produced by combinatorial chemical synthesis orother methods can be tested (see e.g., Ohlmeyer, M. H. J. et al., Proc.Natl. Acad. Sci. USA 90:10922-10926 (1993) and DeWitt, S. H. et al.,Proc. Natl. Acad. Sci. USA 90:6909-6913 (1993), relating to taggedcompounds; see also, Rutter, W. J. et al., U.S. Pat. No. 5,010,175;Huebner, V. D. et al., U.S. Pat. No. 5,182,366; and Geysen, H. M., U.S.Pat. No. 4,833,092). Where compounds selected from a combinatoriallibrary by the present method carry unique tags, identification ofindividual compounds by chromatographic methods is possible. Wherecompounds do not carry tags, chromatographic separation, followed bymass spectrophotometry to ascertain structure, can be used to identifyindividual compounds selected by the method, for example.

An in vivo assay useful to identify drugs which act selectively onarteries or on veins is also available. It is carried out usingtransgenic animals, such as those described herein, which make itpossible to visualize angiogenic processes. For example, an EphrinB2knockout mouse containing a marker, such as a tau-lacZ insertion, thatmarks all arteries but not veins, can be used for a variety of in vivoassays. Other marker genes that can be used, for instance, are genesexpressing alkaline phosphatase, blue fluorescent protein or greenfluorescent protein. The mouse, or the targeted allele it contains, canbe used to study angiogenic processes, such as tumor angiogenesis andischemia-associated cardiac neovascularization, in arteries, independentof veins. For example, tumor cells can be implanted in the indicatormouse and arterial vessel growth into the tumor can be visualized bylacZ staining. Alternatively, mice bearing the targeted allele can becrossed with a mouse model of another condition, such as vasculardegeneration or neovascularization, to be visualized. Thearterial-specific aspects of the process can be visually monitored bylacZ staining. An indicator of this type can also be used to assessdrugs for their angiogenic or anti-angiogenic effects.

A gene product produced specifically by arterial endothelial cells(arteries) and not by other cell types allows for the specific targetingof drugs, diagnostic agents, tagging labels, histological stains orother substances specifically to arteries. In an analogous manner, agene product identified as produced specifically by venous endothelialcells (veins) and not detectably produced by other cell types allows forthe specific targeting and delivery of drugs, diagnostic agents, tagginglabels, histological stains or other substances specifically to veins.The following description of targeting vehicles, targeted agents andmethods is presented using EphrinB2 as an illustration of a gene productproduced by arterial endothelial cells and not by vein cells and EphB4as an illustration of a gene product produced by venous endothelialcells and not by artery cells. However, this description applies equallywell to other artery-specific and vein-specific gene products that canbe used to identify these tissue types.

The differential expression of EphrinB2 in arteries and of Eph4 in veinsallows for the specific targeting of drugs, diagnostic agents, imagingagents, or other substances to the cells of arteries or of veins. Atargeting vehicle can be used for the delivery of such a substance.Targeting vehicles which bind specifically to EphrinB2 or to Eph4 can belinked to a substance to be delivered to the cells of arteries or veins,respectively. The linkage can be via one or more covalent bonds, or byhigh affinity non-covalent bonds. A targeting vehicle can be anantibody, for instance, or other compound which binds either to EphrinB2or to EphB4 with high specificity. Another example is an aqueouslysoluble polypeptide having the amino acid sequence of the extracellulardomain of EphB4, or a sufficient portion of the extracellular domain (ora polypeptide having an amino acid sequence conferring a similar enoughconformation to allow specific binding to EphrinB2), which can be usedas a targeting vehicle for delivery of substances to EphrinB2 inarteries. Similarly, a soluble polypeptide having the amino acidsequence of the extracellular domain of EphrinB2 or a sufficientantigenic portion of the extracellular domain (or a polypeptide havingan amino acid sequence conferring a similar enough conformation to allowspecific binding to EphB4), can be used to target substances to EphB4 inveins.

Targeting vehicles specific to an artery-specific Ephrin ligand (e.g.,EphrinB2) or to a vein-specific Eph receptor (e.g., EphB4) have in vivo(e.g., therapeutic and diagnostic) applications. For example, anantibody which specifically binds to EphrinB2 can be conjugated to adrug to be targeted to arteries (e.g., a therapeutic, such as ananti-plaque agent). Alternatively, an antibody which specifically bindsto EphB4 can be used to target a drug to veins. A substance (e.g., aradioactive substance) which can be detected (e.g., a label) in vivo canalso be linked to a targeting vehicle which specifically binds to anartery-specific Ephrin ligand (e.g., EphrinB2) and the conjugate can beused as a labeling agent to identify arteries. Similarly, a detectablelabel can be linked to a targeting vehicle which specifically binds avein-specific Eph receptor (e.g., EphB4) to identify veins.

Targeting vehicles specific to EphrinB2 or to EphB4 find furtherapplications in vitro. For example, an EphB4-specific targeting vehicle,such as an antibody (a polyclonal preparation or monoclonal) whichspecifically binds to EphB4, can be linked to a substance which can beused as a stain for a tissue sample (e.g., horseradish peroxidase) toprovide a method for the identification of veins in a sample. Likewise,an antibody which specifically binds to EphrinB2 or to the extracellulardomain of EphrinB2 can be used in the identification of arteries. Forinstance, in a biopsied tissue sample, as from a tumor, or from anarteriovenous malformation in a child or adult, antibody to EphrinB2 orto the extracellular domain of EphrinB2 can be used to identify arterytissue and to distinguish it from vein tissue.

To treat malformed, painful or cosmetically undesirable veins, an agentwhich acts against them (e.g, antiangiogenic factors) can be linked toan EphB4-specific vehicle for local administration to the veins. Forexample, anti-angiogenic factors can be injected into varicose veins.

Targeted agents directed to either an artery-specific Ephrin familyligand (e.g., EphrinB2) or a vein-specific Eph family receptor (e.g.,EphB4) can also be used when it is desired to produce an effect on botharteries and veins. For example, limited amounts of targeted agentscomprising an anti-angiogenic drug and a targeting vehicle to eitherEphrinB2, EphB4, or both, can be administered locally to sites ofangiogenesis, such as sites of tumor formation or sites of undesirableneovascularization where it is desired to inhibit the growth of bloodvessels, or to areas in which increased vascularization is desired toenhance growth or establishment of blood vessels.

Substances that act as agonists or antagonists of an artery-specificEphrin family ligand (e.g., EphrinB2) or a vein-specific Eph familyreceptor (e.g., EphB4) can be used as angiogenic or anti-angiogenicagents. Drugs that target these molecules will selectively influencearterial and venous angiogenesis. For example, monoclonal antibodies toEphrinB2 or EphB4 can serve as artery- or vein-specific angiogenic oranti-angiogenic agents. Drugs that interfere with EphrinB2 function (forinstance, blocking antibodies) can be used in anti-angiogenic methods oftherapy. As can be concluded from the phenotype shown by theEphrinB2^(tlacZ)/EphrinB2^(tlacZ) mutant mice, antagonists of EphrinB2or antagonists of EphB4 will inhibit angiogenesis. Agents which areagonists of both EphrinB2 and EphB4 will promote angiogenesis.

In another example, soluble agonists which comprise the extracellulardomain of an Ephrin family ligand or the extracellular domain of an Ephfamily receptor fused to the Fc domain of human IgG can be produced. Forexample, an EphB4 or an EphrinB2 hybrid protein in which theextracellular domain of the membrane protein is fused to the Fc domainof human IgG can be used (Wang, H. U. and D. J. Anderson, Neuron18:383-396 (1997)). See, for examples of methods Stein, E. et al., Genesand Dev. 12:667-678 (1998), regarding experiments on responses of cellsto clustered Ephrin-B1/Fc fusion proteins. Clustering of these hybridmolecules with anti-human Fc antibodies generates soluble agonists:Ephrin-derived “ligand-bodies” for Eph receptors, and conversely,Eph-derived “receptor bodies” for Ephrins. Non-clustered forms of thesehybrid molecules can be used as antagonists.

A further application of isolated arterial endothelial cells andisolated venous endothelial cells is the genetic alteration of theisolated cells and the administration of these cells, preferablyintravenously, to the host mammal from which the cells were isolated, orinto another compatible host, where the cells can be incorporated into ablood vessel of the appropriate type. In this way, the effects of agenetic defect which is manifested in arteries or in veins can beameliorated. It has been demonstrated that circulating endothelial cellprogenitors can migrate to sites of neovascularization and beincorporated into blood vessels (Asahara et al., Science 275:964-967(1997)).

The introduction of a gene (an endogenous gene that has been altered, ora gene originally isolated from a different organism, for example) intocells can be accomplished by any of several known techniques, forexample, by vector mediated gene transfer, as by amphotropicretroviruses, calcium phosphate, or liposome fusion, for example.

A gene intended to have an effect on arteries or veins in a host mammalcan be delivered to isolated artery cells or isolated vein cells by theuse of viral vectors comprising one or more nucleic acid sequencesencoding the gene of interest. Generally, the nucleic acid sequence hasbeen incorporated into the genome of the viral vector. In vitro, theviral vector containing the nucleic acid sequences encoding the gene canbe contacted with a cell and infection can occur. The cell can then beused experimentally to study, for example, the effect of the gene ongrowth of artery or vein cells in vitro or the cells can be implantedinto a patient for therapeutic use. The cells to be altered byintroduction or substitution of a gene can be present in a biologicalsample obtained from the patient and used in the treatment of disease,or can be obtained from cell culture and used to dissect developmentalpathways of arteries and veins in in vivo and in vitro systems.

After contact with the viral vector comprising a nucleic acid sequenceencoding the gene of interest, the treated artery or vein cells can bereturned or readministered to a patient according to methods known tothose practiced in the art. Such a treatment procedure is sometimesreferred to as ex vivo treatment. Ex vivo gene therapy has beendescribed, for example, in Kasid, et al., Proc. Natl. Acad. Sci. USA87:473 (1990); Rosenberg, et al., New Engl. J. Med. 323:570 (1990);Williams, et al., Nature 310476 (1984); Dick, et al., Cell 42:71 (1985);Keller, et al., Nature 318:149 (1985) and Anderson, et al., U.S. Pat.No. 5,399,346 (1994).

Generally, viral vectors which can be used therapeutically andexperimentally are known in the art. Examples include the vectorsdescribed by Srivastava, A., U.S. Pat. No. 5,252,479 (1993); Anderson,W. F., et al., U.S. Pat. No. 5,399,346 (1994); Ausubel et al., “CurrentProtocols in Molecular Biology”, John Wiley & Sons, Inc. (1998).Suitable viral vectors for the delivery of nucleic acids to cellsinclude, for example, replication defective retrovirus, adenovirus,parvovirus (e.g., adeno-associated viruses), and coronavirus. Examplesof retroviruses include avian leukosis-sarcoma, mammalian C-type, B-typeviruses, lentiviruses (Coffin, J. M., “Retroviridae: The Viruses andTheir Replication”, In: Fundamental Virology, Third Edition, B. N.Fields, et al., eds., Lippincott-Raven Publishers, Philadelphia, Pa.,(1996)). The mechanism of infectivity depends upon the viral vector andtarget cell. For example, adenoviral infectivity of HeLa cells occurs bybinding to a viral surface receptor, followed by receptor-mediatedendocytosis and extrachromasomal replication (Horwitz, M. S.,“Adenoviruses” In: Fundamental Virology, Third Edition, B. N. Fields, etal., eds., Lippincott-Raven Publishers, Philadelphia, Pa., (1996)).

The present invention is illustrated by the following examples, whichare not intended to be limiting in any way.

EXAMPLES

Experimental Procedures

The following experimental procedures were used in the examples whichfollow.

Targeted disruption of the EphrinB2 gene. A 200 base pair probe startingfrom the ATG of the mouse EphrinB2 gene (Bennett, B. D., et al., Proc.Natl. Acad. Sci. USA 92:1866-1870 (1995)) was used to screen a 129SVJgenomic library (Stratagene). Analysis of several overlapping clonesrevealed that the first exon, including the signal sequence, ends at 131base pairs after the ATG. Further phage analysis and library screensrevealed that the rest of the EphrinB2 gene was located at least 7 kbdownstream from the first exon. To construct a targeting vector (FIG.1B), a 3 kb Xbal-NcoI fragment whose 3′ end terminated at the ATG wasused as the 5′ arm. A 5.3 kb Tau-lacZ coding sequence (Mombaerts, P., etal., Cell 87:675-686 (1996)) was fused in frame after the ATG. ThePGKneo gene (Ma, Q., et al., Neuron 20:469-482 (1998)) was used toreplace a 2.8 kb intronic sequence 3′ to the first exon. Finally, a 3.2kb downstream EcoRI-EcoRI fragment was used as the 3′ arm. Normal (6 kb)and targeted (9 kb) loci are distinguished by HindIII digestion whenprobed with a 1 kb HindIII-XbaI genomic fragment. Electroporation,selection and blastocyst-injection of AB-1 ES cells were performedessentially as described Ma, Q., et al. (Neuron 20:469-482 (1998)), withthe exception that FIAU-selection was omitted. ES cell targetingefficiency via G418 selection was 1 out of 18 clones. Germlinetransmission of the targeted EphrinB2 locus (FIG. 1C) in heterzygousmales was confirmed by Southern blotting of tail DNA of adult mice,using a 1 kb HindIII-XbaI probe. Subsequent genotyping was done bygenomic PCR. Primers for Neo are

-   5′-AAGATGGATTGCACGCAGGTTCTC-3′ (SEQ ID NO.: 1) and-   5′-CCTGATGCTCTTCGTCCAGATCAT-3′ (SEQ ID NO.: 2). Primers for the    replaced intronic fragment are-   5′-AGGACGGAGGACGTTGCCACTAAC-3′ (SEQ ID NO.: 3) and-   5′-ACCACCAGTTCCGACGCGAAGGGA-3′ (SEQ ID NO.: 4).

LacZ, PECAM-1, and histological staining. Embryos and yolk sacs wereremoved between E7.5 and E10.0, fixed in cold 4% paraformaldehyde/PBSfor 10 minutes, rinsed twice with PBS, and stained for 1 hour toovernight at 37° C. in X-gal buffer (1.3 mg/ml potassium ferrocyanide, 1mg/ml potassium ferricyanide, 0.2% Triton X-100, 1 mM MgCl₂, and 1 mg/mlX-gal [5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside] in PBS, pH7.2). LacZ stained embryos were post-fixed and photographed, orsectioned on a cryostat after embedding in 15% sucrose and 7.5% gelatinin PBS. Procedures for whole mount or section staining with anti-PECAM-1antibody (clone MEC 13.3, Pharmingen) were done essentially as describedMa et al (Neuron 20:469-482 (1998); Fong et al., Nature 376:66-70(1995)). Horseradish peroxidase-conjugated secondary antibodies wereused for all PECAM-1 stainings. LacZ-stained yolk sacs were sectioned ingelatin and then subjected to hematoxylin counter-staining by standardprocedures.

In situ hybridization. In situ hybridization on frozen sections wasperformed as previously described (Birren et al. Development 119:597-610(1993)). Whole-mount in situ hybridization followed a protocol byWilkinson, D. G., (Whole-mount in situ hybridization of vertebrateembryos. pp. 75-83 In: In Situ Hybridization: A Practical Approach (ed.D. G. Wilkinson) IRL Press, Oxford: 75-83 (1992). Bluescript vectors(Stratagene) containing cDNAs for EphB2/Nuk and EphB4/Myk-1 weregenerated as described Wang, H. U. and Anderson, D. J. (Neuron18:383-396 (1997)).

Example 1 Targeted Mutagenesis of EphrinB2 in Mice

Targeted disruption of the EphrinB2 gene was achieved by homologousrecombination in embryonic stem cells. The targeting strategy involveddeleting the signal sequence and fusing a tau-lacZ indicator gene inframe with the initiation codon. The expression pattern ofβ-galactosidase in heterozygous (EphrinB2^(tlacZ/+)) embryos wasindistinguishable from that previously reported for the endogenous gene.(Bennett, B. D. et al. Proc. Natl. Acad. Sci. USA 92: 1866-1870 (1995);Bergemann, A. D. et al. Mol. Cell. Bio. 1995:4921-4929 (1995); Wang, H.U. and Anderson, D. J. Neuron 18:383-396 (1997)). While prominentexpression was detected in the hindbrain and somites, lower levels wereobserved in the aorta and heart as early as E8.25. Expression in theyolk sac was first detected at E8.5. Heterozygous animals appearedphenotypically normal. In homozygous embryos, growth retardation wasevident at E10 and lethality occurred with 100% penetrance around E11.No expression of endogenous EphrinB2 mRNA was detected by in situhybridization, indicating that the mutation is a null. Somite polarity,hindbrain segmentation, and the metameric patterning of neural crestmigration (in which EphrinB2 and related ligands have previously beenimplicated Xu, W. et al. Development 121:4005-4016 (1995); Wang, H. U.and Anderson, D. J. Neuron 18:383-396 (1997); Krull, C. E. et al. Curr.Biol. 7:571-580 (1997); Smith, A. et al. Curr. Biol. 7:561-570 (1997))appeared grossly normal in homozygous mutant embryos.

Example 2 Reciprocal Expression Pattern of EphrinB2 and EphB4 inArteries and Veins

The enlarged heart observed in dying mutant embryos prompted examinationof the expression of EphrinB2^(tlacZ) in the vascular system in detail.Expression was consistently observed in arteries but not veins. In theyolk sac, for example, the posterior vessels connected to the vitellineartery, but not the vitelline vein, expressed the gene, as detected bylacZ staining. In the trunk, labeling was detected in the dorsal aorta,vitelline artery, umbilical artery and its allantoic vascular plexus,but not the umbilical, anterior and common cardinal veins (the umbilicalvein is labeled with anti-PECAM-1 antibody). In the head, labeling wasseen in branches of the internal carotid artery, but not in those of theanterior cardinal vein. In situ hybridization with EphrinB2 cDNA probesconfirmed that the selective expression of tau-lacZ in arteriescorrectly reflected the pattern of expression of the endogenous gene.Examination of the expression of the four EphB family genes, as well asEph A4/Sek1, which are receptors for EphrinB2 Gale, N. W. et al., Neuron17:9-19 (1996) revealed complementary expression of EphB4 in veins butnot arteries, including the vitelline vein and its branches in anteriorportion of the yolk sac.

Example 3 Vasculogenesis occurs Normally in EphrinB2 Mutant Embryos

The formation of the major vessels in the trunk was unaffected by thelack of EphrinB2, as examined by lacZ and PECAM-1 double staining of 9somite embryos. Expression of EphrinB2-lacZ was seen in the dorsal aortaand vitelline artery, but not the umbilical and posterior cardinalveins. The dorsal aorta, vitelline artery, posterior cardinal andumbilical veins, for example, formed, although some dilation andwrinkling of the vessel wall was observed. Similarly the intersomiticvessels originating from the dorsal aorta formed at this stage. BetweenE8.5 and E9.0, the primitive endocardium appeared only mildly perturbedin mutants, while a pronounced disorganization was apparent at E10. Redblood cells developed and circulated normally up to E9.5 in both themutant yolk sac and embryo proper.

Example 4 Extensive Intercalation of Yolk Sac Arteries and VeinsRevealed by EphrinB2 Expression

In the yolk sac, the vitelline artery and its capillary network occupythe posterior region, and the vitelline vein and its capillaries theanterior region. At E8.5, a stage at which the primary capillary plexushas formed but remodeling has not yet occurred, asymmetric expression ofEphrinB2-taulacZ in heterozygous embryos was evident at the interfacebetween the anterior and posterior regions. Apparently homotypicremodeling of β-galactosidase arterial capillaries into larger, branchedtrunks clearly segregated from venous vessels was evident between E9.0and E9.5. At this stage, expression of the receptor EphB4 was clearlyvisible on the vitelline veins but not arteries. Thus arterial andvenous endothelial capillaries are already molecularly distinctfollowing vasculogenesis and prior to angiogenesis.

While textbook diagrams (Carlson, B. M Patten's Foundations ofEmbryology (1981)) of the yolk sac capillary plexus depict anon-overlapping boundary between the arterial and venous capillary beds,expression of EphrinB2-taulacZ allowed detection of apreviously-unrecognized extensive intercalation between arteries andveins across the entire anterior-posterior extent of the yolk sac; thiswas observed in the heterozygote, but not in the homozygote.Double-labeling for PECAM and β-galactosidase revealed that theinterface between the arteries and veins occurs between microvesselextensions that bridge larger vessels interdigitating en passant.

Example 5 Disrupted Angiogenesis in the Yolk Sac ofEphrinB2^(tlacZ)/EphrinB2^(tlacZ) Embryos

Defects in yolk sac angiogenesis was were apparent by E9.0 and obviousat E9.5. There was an apparent block to remodeling at the capillaryplexus stage, for both arterial vessels as revealed by β-galactosidasestaining and venous vessels in the anterior region of the sac asrevealed by PECAM staining. Thus, disruption of the EphrinB2 ligand genecaused both a non-autonomous defect in EphB4 receptor-expressing venouscells, and an autonomous defect in the arteries themselves.

This defect was accompanied by a failure of intercalating bi-directionalgrowth of arteries and veins across the antero-posterior extent of theyolk sac, so that an interface between EprhinB2-expressing andnon-expressing zones at the midpoint of the sac was apparent. (However,small patches of lacZ expression were occasionally visible within theanterior venous plexus, suggesting that some arterial endothelial cellsmay have become incorporated into venous capillaries.) Theseobservations imply a close relationship between the remodeling of thecapillary plexus into larger vessels and the intercalating growth ofthese vessels. The large β-galactosidase⁺ vitelline arteries as well asvitelline veins present at the point of entry to the yolk sac of theembryo-derived vasculature appeared unperturbed in the mutant, however.This is consistent with the observation that the mutation does notaffect formation of the primary trunk vasculature. It also argues thatthe yolk sac phenotype is due to a disruption of intrinsic angiogenesisand is not secondary to a failure of ingrowth of embryo-derived vessels.

Histological staining (hematoxylin) of sectioned yolk sacs revealed anaccumulation of elongated support cells (mesenchymal cells or pericytes)in close association with the endothelial vessels at E10 and E10.5. Inmutant yolk sacs, these support cells appeared more rounded, suggestinga defect in their differentiation. Moreover, in contrast to heterozygousyolk sacs, where vessels of different diameters began to appear at E9.5and vessel diameter increased through E10.5, capillary diameter appearedrelatively uniform and did not increase with age in the mutants. AtE10.5, arteries appear dilated, as if fusion of vessels occurred withoutencapsulation by support cells. The mutant capillaries also failed todelaminate from the basal endodermal layer.

Example 6 Absence of Internal Carotid Arterial Branches and DefectiveAngiogenesis of Venous Capillaries in the Head of Mutant Embryos

Similar to the yolk sac phenotype, the capillary bed of the headappeared dilated in the mutant, and apparently arrested at the primaryplexus stage. Staining for β-galactosidase revealed that theanterior-most branches of the internal carotid artery failed to developin the mutant. Unlike the case in the yolk sac, therefore, the malformedcapillary beds must be entirely of venous origin. However the anteriorbranches of the anterior cardinal vein formed although they wereslightly dilated. Taken together, these data indicate that in the head,venous angiogenesis is blocked if the normal interaction with arterialcapillaries is prevented. The angiogenic defects observed in the headand yolk sac are unlikely to be secondary consequences of heart defects(see below), since they are observed starting at E9.0 and the embryonicblood circulation appears normal until E9.5.

Example 7 EphrinB2-Dependent Signaling Between Endocardial Cells isRequired for Myocardial Trabeculae Formation

Examination of ligand and receptor expression in wild-type heartsrevealed expression in the atrium of both EphrinB2 (as detected by lacZstaining) and EphB4 (as detected by in situ hybridization). Expressionof both ligand and receptor was also detected in the ventricle in theendocardial cells lining the trabecular extensions of the myocardium.Double-labeling experiments suggested that the ligand and receptor areexpressed by distinct but partially overlapping cell populations,although the resolution of the method does not permit us to distinguishwhether this overlap reflects co-expression by the same cells, or aclose association of different cells. In any case, expression ofEphrinB2 and EphB4 does not define complementary arterial (ventricular)and venous (atrial) compartments of the heart, unlike the extra-cardiacvasculature.

Heart defects commenced at E9.5 and were apparent in mutant embryos atE10 both morphologically and by wholemount PECAM-1 staining. Sectionsrevealed an absence of myocardial trabecular extensions, althoughstrands of EphrinB2-expressing endocardial cells were still visible.Thus, mutation of the ligand-encoding gene caused a non-autonomousdefect in myocardial cells, similar to the effect of a mutation in theneuregulin-1 gene. (Meyer, D. and Birchmeier, C, Nature 378:386-390(1995)) Paradoxically, however, in this case the EphB4 receptor isexpressed not on myocardial cells, as is the case for the neuregulin-1receptors erbB2 and erbB4 (Lee et al., Nature 378:394-398 (1995);Gassmann, et al., Nature 378:390-394 (1995), but rather on endocardialcells. Expression of any of the other receptors for Ephrin B familyligands (Eph B1, B2, B3 and A4) was detected in this tissue. Thissuggests that in the heart, ligand-receptor interactions amongendothelial cells may in turn affect interactions with smooth musclecells.

Example 8 Ephrin B2 is Required for Vascularization of the Neural Tube

In EphrinB2^(tlacZ)/EphrinB2^(tlacZ) embryos capillary ingrowth into theneural tube failed to occur. Instead, EphrinB2-expressing endothelialcells remained associated with the exterior surface of the developingspinal cord. Comparison of β-galactosidase to pan-endothelial PECAM-1and EphB4 expression provided no evidence of a separate, venouscapillary network expressing EphB4 in the CNS at this early stage(E9-E10). Rather, expression of a different EphrinB2 receptor, Eph B2,was seen in the neural tube as previously reported Henkemeyer, et al.,Oncogene 9:1001-1014 (1994), where no gross morphological or patterningdefects were detectable. In this case, therefore, the mutation does notappear to cause a non-autonomous phenotype in receptor-expressing cells,rather only an autonomous effect on ligand-expressing cells.

Example 9 EphrinB2 is Artery-Specific in Adult Tissues

To determine whether ephrin-B2 is expressed in adult tissues in anartery-specific manner, we performed histochemical staining forβ-galactosidase on ephrin-B2^(taulacZ)/+ heterozygous mice. Antibodystaining for PECAM-1, a pan-endothelial marker, was performed on thesame or on adjacent sections to reveal non-arterial vessel (i.e.,veins). Ephrin-B2 is expressed throughout the adult mouse in anartery-specific manner, in tissues including the heart, leg muscle,kidney, liver and fat. Expression was detected in vessels of alldiameters, including large arteries, arterioles and thesmallest-diameter capillaries. It had been previously assumed thatcapillaries by definition have neither arterial nor venous identity.These results show that this is not the case, and that arterial identityextends into the capillary beds.

Sections through adult arteries were double labeled by histochemicalstaining for β-galactosidase (lacZ) to reveal ephrin-B2-taulacZexpression, and with antibody to PECAM-1 as a pan-endothelial marker.LacZ (blue from X-gal) staining revealed ephrinB2 expression in dorsalaorta but not in inferior vena cava, in femoral artery next to the legbone, but not in femoral vein, and in coronary epicardial artery, butnot in coronary vein.

Similar staining of other sections revealed the presence of EphrinB2 inkidney arteriole, liver arteriole and small muscle arteriole, as well asarterial capillary. Kidney venule, hepatic vein, and muscle veins werelacZ-negative but PECAM-1 positive.

Gut fat was stained for lacZ (β-galactosidase) and labeled with PECAM-1to reveal venous vessels as well as arterial vessels. EphrinB2 isexpressed by arterioles and arterial capillaries and in arteriole butnot in PECAM-1 positive venule. A further section showed that EphrinB2is expressed by arterial capillaries surrounded by PECAM-1 positivenon-arterial capillaries.

Example 10 Ephrin-B2 is Expressed during Tumor Angiogenesis

It had been assumed that tumor vessels sprout from the post-capillaryvenules. To address the question of whether EphrinB2 is expressed duringtumor angiogenesis, Lewis Lung Carcinomas were implanted subcutaneouslyin the dorsal region of ephrin-B2^(taulacZ)/+ heterozygous females.After one week, the tumors were removed and processed forβ-galactosidase histochemistry in whole mounts. The results indicateclearly that ephrin-B2 is in fact expressed by tumor vessels. This wasconfirmed by double-staining of sections cut through such tumors, forβ-galactosidase and PECAM-1.

EphrinB2 expression by tumor capillaries. Lewis Lung Carcinoma (LLC)cells were implanted subcutaneously in the dorsal region ofEphrinB2-taulacZ heterozygous females. After one week, tumors wereremoved for staining. EphrinB2 positive arterial capillaries wereobserved in peripheral tumor tissue. Double labeling with PECAM-1colocalized the EphrinB2 lacZ (staining blue) and PECAM-1 (stainingbrown) signals in arterial capillaries, and reveals non-arterialcapillaries labeled by PECAM-1 only.

Example 11 Screen for Clones Containing Artery-Specific Genes

A summary of the screening procedures used is provided in Appendix I.Briefly, endothelial cells were isolated from dissociated embryonic yolksac, vitelline arteries or vitelline veins using positive selection withantibody to PECAM-1 (magnetic bead or FACS). cDNA was synthesized fromlysates of either single cells or small numbers (ca. 200) of cells, andamplified by PCR. To confirm that the cDNAs were from arterial or venousendothelial cells, the cDNA synthesized from each cell prep was Southernblotted and hybridized in quadruplicate with a series of probes,including tubulin (ubiquitously expressed) the pan-endothelial probesFlk1 and Flt1, and the arterial-specific probe ephrin-B2. cDNAs thatcontained Flk1, Flt1 and ephrin-B2 sequences were considered arterial,while those that contained the pan-endothelial markers but not ephrin-B2were considered venous. Thus the use of ephrin-B2 probes in thisprocedure was essential to confirm the arterial vs. venous nature of thecDNAs synthesized.

To isolate additional arterial-specific genes from these cDNAs, theywere cloned into a phage lambda vector to generate cDNA libraries.Plaques from these libraries were then screened in duplicate filterlifts with arterial- or venous-specific cDNA probes made from eithersingle cells or pools of cells. Plaques exhibiting differentialhybridization to the arterial vs. venous probes were isolated, and theinserts were amplified using T3-T7 primers, and re-analyzed by cDNASouthern blotting. Two different pairs of arterial-venous endothelialcell cDNA probes (vitelline artery-vein cells and single yolk sacarterial and venous endothelial cells) were used in the Southern blot.Most of the clones were strongly expressed in arterial cells, andexpressed weakly or not detectably by venous cells. The initial screenwas designed to isolate additional arterial-specific genes. Twelvecandidate arterial-specific clones were isolated using the single-cellprobes, while one clone was isolated using the pooled probe. Thearterial-specific expression of these genes in vivo can be confirmed byin situ hybridization experiments. Methods such as these can be appliedto arterial endothelial cells or vein-specific cells.

These data show that it will be possible to isolate novel arterial- orvenous-specific genes from single endothelial cells. Such vesseltype-restricted genes may provide insights into the physiologicaldifferences between arterial and venous endothelial cells. Methods suchas those described herein can also identify genes involved in theetiology of arterial and venous specific diseases, such as arterialhypertension, atherosclerosis, deep venous thrombosis, and certain typesof venous malformations. They can also provide candidate genes for humangenetic disorders of the circulatory system. The gene products of suchgenes can then serve as novel drug targets.

Appendix I: Single Cell PCR, 3′ cDNA Library Construction AndDifferential Screening Procedure to Isolate Novel Arterial- orVenous-Specific Genes

-   -   1. Dissection of vitelline arteries and vitelline veins from        E12.5 to E14.5 yolk sacs, based on morphological criteria.    -   2. Dissociation of yolk sacs in collagenase solution (5 mg/ml)        at 37° C. for 45′.    -   3. Isolate single or small groups of endothelial cells (ECs) by        one of the following methods.        -   a) Magnetic bead-based separation using PECAM-1 as primary            antibody.        -   b) FACS purification using PECAM-1-FITC primary antibody.        -   c) GFP fluorescence from tie2-GFP transgenic mouse for            endothelial cell identification, followed by microcapillary            mouth-pipeting.    -   4. Lyse the single cells in PCR tubes at 65° C. for 1′.    -   5. Keep 1-2′ at room temperature to allow the oligo-T to anneal        to RNA.    -   6. Reverse transcription using AMV and MMLV enzyme mixture, at        37° C. for 15′.    -   7. Poly-A tailing with terminal transferase and dATP, at 37° C.        for 15′.    -   8. PCR reaction set up:        -   100 μl reaction, 5-fold normal level of dNTP mix, high            concentration of Taq.        -   Using a single PCR primer with 24 (T)s at 3′ end for            symmetrical amplification.    -   9. cDNA Southern blotting with endothelial specific and        arterial/venous specific 3′ probes on the amplified cDNAs for        each cell prep.    -   10. Choose a few good cells that give strong signals for the        appropriate probes. Isolate cDNAs from 500 bp to 2 kb on agarose        gel.    -   11. Precipitate and quantify cDNA.    -   12. Ligate into lambda ZAPII (Stratagene; LaJolla, Calif.) phage        arms for cDNA libraries.    -   13. Plate the library at very low density: 1000 pfu/plate. Take        duplicate filter lifts.    -   14. Screen duplicate filters with probes made from vitelline        artery cells and vitelline vein cells.    -   15. Pick differentially expressed phage clones. Reverse (cDNA)        Southern blot confirmation of phage inserts by probing with        probes made from vitelline artery cells and vitelline vein        cells.    -   16. In situ hybridization to examine the expression patterns of        cDNA fragments.

Example 12 Generation of Monoclonal Antibodies against the ExtracellularDomain of Ephrin-B2

While polyclonal rabbit antibodies to fragments of ephrin-B2 expressedin bacteria had previously been reported, such antibodies are typicallynot reactive with native forms of the protein on the cell surface, andtherefore are not useful for many applications including cell sorting,functional inhibition and drug-targeting. To generate antibodies withmore desirable binding properties, we expressed the extracellular domainof ephrin-B2 as a glycophosphatidylinositol (GPI)-linked form on ChineseHamster Ovary (CHO) cells. Hamsters were immunized with these cells,hybridomas prepared by fusion with mouse myeloma cells, and supernatantsscreened on COS cells expressing ephrin-B2-GPI.

Supernatant from clone #6E3 bound well to ephrinB2 on live COS cells.The ephrin-B2-GPI COS cell lines are a pooled population ofG418-selected cells, with 30% of the cells being positive for ephrinB2.Control (untransfected) COS cells were negative when stained with thesame antibody.

Example 13 Some Anti-Ephrin-B2 Antibodies Block the EphB2-EphrinB2Binding Interaction

In cases where the antibodies also block function (i.e., inhibit bindingof ephrin-B2 to its receptors), they can be used as potentialanti-angiogenic agents. To demonstrate an assay to identify suchfunction-inhibiting antibodies, we screened 12 hamster anti-EphrinB2hybridoma supernatants for their ability to reduce the binding ofGPI-ephrin-B2 (expressed on COS cells) to a soluble EphB2-Fc fusionprotein. Binding was detected by ¹²⁵I-labeled goat anti-human Fcantibody. Pre-incubation of cells with various supernatants revealedthat the majority of the antibodies have no blocking effects onsubsequent receptor-ligand binding (control as 100%), even though thesesupernatants all contained antibodies that bound to ephrin-B2-GPI. Oneof the antibodies produced a 40% reduction in EphB2-Fc binding to theephrin-B2-GPI COS cells (FIG. 2).

EQUIVALENTS

While this invention has been particularly shown and described withreferences to preferred embodiments thereof, it will be understood bythose skilled in the art that various changes in form and details may bemade therein without departing from the spirit and scope of theinvention as defined by the appended claims. Those skilled in the artwill recognize or be able to ascertain using no more than routineexperimentation, many equivalents to the specific embodiments of theinvention described specifically herein. Such equivalents are intendedto be encompassed in the scope of the claims.

1-76. (canceled)
 77. A method for inhibiting angiogenesis in an adultmammal, comprising administering to the adult mammal, in atherapeutically effective quantity, an antagonist of EphrinB2 or anantagonist of EphB4, wherein the antagonist is selected from the groupconsisting of: i) an antibody which binds to EphrinB2; ii) an antibodywhich binds to EphB4; iii) a soluble antagonist comprising anextracellular domain of EphrinB2; and iv) a soluble antagonistcomprising an extracellular domain of EphB4.
 78. The method of claim 1,wherein the antibody of (i) or (ii) is a polyclonal antibody.
 79. Themethod of claim 1, wherein the antibody of (i) or (ii) is a monoclonalantibody.
 80. The method of claim 1, wherein the soluble antagonist of(iii) and (iv) comprises an Fc domain of a human IgG antibody.
 81. Themethod of claim 1, wherein the soluble antagonist of (iii) and (iv) isin non-clustered form.
 82. The method of claim 1, wherein the agent isadministered locally to a site of angiogenesis.
 83. The method of claim6, wherein the site of angiogenesis is a tumor.
 84. The method of claim6, wherein the mammal is a human.
 85. A method for selectivelydelivering an agent to arteries in an adult mammal, comprisingadministering to the adult mammal a complex comprising: a) an agent; andb) a component which binds to EphrinB2 selected from the groupconsisting of: an antibody which binds to EphrinB2, a solublepolypeptide comprising an extracellular domain of EphB4; and a solublepolypeptide comprising an EphrinB2-binding portion of the extracellulardomain of EphB4, under conditions appropriate for the component of (b)to bind to EphrinB2, whereby the agent is delivered to arteries.
 86. Themethod of claim 9, wherein the agent is an anti-angiogenic agent. 87.The method of claim 9, wherein the agent is an angiogenic agent.
 88. Themethod of claim 9, wherein the agent is selected from the groupconsisting of: a drug, a diagnostic agent, an environmental factor and adietary factor.
 89. The method of claim 9, wherein the agent is ananti-plaque agent.
 90. The method of claim 9, wherein the agent isselected from the group consisting of a growth factor and a cytokine.91. The method of claim 9, wherein the agent is a diagnostic agent. 92.The method of claim 15, wherein the diagnostic agent comprises a labelselected from the group consisting of a radioactive label, a fluorescentlabel, a colorimetric label, an enzyme label, an antigenic label, anepitopic label and a biotin label.
 93. The method of claim 9, whereinthe complex is a fusion protein.
 94. The method of claim 17, wherein thefusion protein comprises a moiety selected form the group consisting ofalkaline phosphatase, blue fluorescent protein, green fluorescentprotein and β-galactosidase.
 95. The method of claim 9, wherein themammal is a transgenic mammal.
 96. The method of claim 9, wherein themammal is a human.